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    FDA 483 for Wyeth BioPharma (Pearl River) Inspection Ending Mar 17, 2017 (FEI 2410662)

    FDA 483 for Wyeth BioPharma (Pearl River) Inspection Ending Mar 17, 2017 (FEI 2410662)

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    $69.00 USD
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    Original Request: To Whom it May Concern: As permitted by the Freedom of Information Act (FOIA), I am hereby requesting the following document: Form FDA 483 Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC Pearl River, United States of America End Dates of inspection: 17 Mar 2017 Project Area: Drug Quality Assurance FEI: 2410662 Investigator(s): Maria Joselopez Barragan, PhD, Diane L Raccasi, Antonina Aydanian, Mate Tolnay, Marjorie A Shapiro, PhD, Wayne E Seifert, Charles Jewell Classification: VAI
    Tags: Pharma, 483, 2017
    • Status: Pending Fast-Track Request
    • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

    NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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